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FDA 510(k)

MONOSTERYL

K-Number: K926205 · 1994-02-10

ApplicantUtensili Super Abrasivi
Decision Date1994-02-10
Product CodeEJL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MONOSTERYL is the device name listed in this FDA 510(k) record. The listed applicant is Utensili Super Abrasivi. It received FDA 510(k) clearance on 1994-02-10 under 510(k) number K926205. The device is classified under product code EJL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOSTERYL?

MONOSTERYL is a medical device that received FDA 510(k) clearance on 1994-02-10. The listed applicant is Utensili Super Abrasivi. The 510(k) number is K926205.

When did MONOSTERYL receive FDA 510(k) clearance?

MONOSTERYL received FDA 510(k) clearance on 1994-02-10, under 510(k) number K926205.

Who is the listed applicant for MONOSTERYL?

The FDA 510(k) record lists Utensili Super Abrasivi as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONOSTERYL?

The FDA product code for MONOSTERYL is EJL.

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Related Devices (Code: EJL)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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